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filingDate 2012-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_565ef3f1d6714309e1224acf7064b223
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publicationDate 2017-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber NZ-713390-A
titleOfInvention New compounds for treating, delaying and/or preventing a human genetic disorder such as myotonic dystrophy type 1 (dm1)
abstract Discloses compounds comprising or consisting of the oligonucleotide sequence (NAG)m, wherein N is C or 5-methylcytosine and at least one occurrence of N is 5- methylcytosine and wherein m is 7, 8, 9, 10, 11, 12, 13, 14, or 15 and wherein no inosine nucleotide is present. Also discloses use of compound to treat dystrophy type 1, spino-cerebellar ataxia 8 and/or Huntington’s disease-like 2 caused by expansion of CUG repeats.
priorityDate 2011-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9V1P1
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424905654
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414021769
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559233
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP27726
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID416067515
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID73188
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCA4WIW2
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ06163
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID100136352
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCA6VIW4
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID46891827
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Total number of triples: 423.